Variant report

Variant	rs6746367
Chromosome Location	chr2:187439293-187439294
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:187438845..187441409-chr2:187470852..187472926,2	K562	blood:
2	chr2:187406154..187410015-chr2:187435632..187441776,6	MCF-7	breast:
3	chr2:187437479..187442784-chr2:187443924..187447436,6	MCF-7	breast:
4	chr2:187438759..187442258-chr2:187444014..187446139,4	MCF-7	breast:
5	chr2:187432930..187434820-chr2:187437011..187439461,2	MCF-7	breast:
6	chr2:187406067..187412442-chr2:187438004..187442761,8	MCF-7	breast:
7	chr2:187435611..187437376-chr2:187439116..187441984,2	MCF-7	breast:
8	chr2:187438412..187440075-chr2:187442178..187444992,2	K562	blood:

No data

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10153708	0.83[AMR][1000 genomes]
rs10191572	0.83[AMR][1000 genomes]
rs10191888	0.83[AMR][1000 genomes]
rs10196722	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10202802	0.83[AMR][1000 genomes]
rs13386665	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13396060	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13403385	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13405296	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13410314	0.83[AMR][1000 genomes]
rs13419307	0.83[AMR][1000 genomes]
rs16828044	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16828048	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16828049	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56316122	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56385600	0.83[AMR][1000 genomes]
rs59828675	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6758885	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73044325	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73044336	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73044342	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73979316	0.83[AMR][1000 genomes]
rs73981329	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73981332	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73981336	0.83[AMR][1000 genomes]
rs9973427	1.00[AFR][1000 genomes]
rs9973506	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9973742	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757844	chr2:187332780-187580547	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv2759107	chr2:187332780-187580547	Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv459988	chr2:187364878-187440683	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv584031	chr2:187364878-187440683	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv1004309	chr2:187389880-187455946	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv536082	chr2:187389880-187455946	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv875552	chr2:187393729-187505486	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv1014203	chr2:187413781-187477586	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
9	nsv536083	chr2:187413781-187477586	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
10	esv2756507	chr2:187416494-187470494	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
11	esv2756956	chr2:187416599-187492742	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
12	nsv818105	chr2:187423298-187481835	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
13	esv2753217	chr2:187424494-187470494	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
14	nsv10208	chr2:187436719-187443357	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187426600-187441200	Weak transcription	Aorta	Aorta
2	chr2:187435200-187439800	Weak transcription	HSMMtube	muscle
3	chr2:187435400-187439400	Weak transcription	Fetal Intestine Small	intestine
4	chr2:187435400-187439600	Weak transcription	HSMM	muscle
5	chr2:187435600-187439800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr2:187435600-187441400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:187435600-187453800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr2:187435800-187439400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:187435800-187439400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:187435800-187439400	Weak transcription	HUVEC	blood vessel
11	chr2:187435800-187439600	Weak transcription	K562	blood
12	chr2:187435800-187439800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:187435800-187439800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr2:187435800-187440400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr2:187435800-187440600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:187436000-187439400	Weak transcription	Osteobl	bone
17	chr2:187436000-187439600	Weak transcription	HepG2	liver
18	chr2:187436000-187439800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr2:187436000-187439800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr2:187436400-187439800	Weak transcription	Hela-S3	cervix
21	chr2:187437800-187439400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr2:187438000-187439600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:187438200-187439400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:187438200-187439400	Enhancers	A549	lung
25	chr2:187438200-187439400	Weak transcription	NHEK	skin
26	chr2:187438200-187439600	Weak transcription	HMEC	breast
27	chr2:187438200-187440000	Weak transcription	Stomach Mucosa	stomach
28	chr2:187438200-187440400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr2:187438400-187439400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:187438600-187439800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:187438600-187448600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:187439200-187442400	Enhancers	NH-A	brain

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